Objective: Review the acute and late results of percutaneous transluminal c
oronary angioplasty (PTCA) in heart transplant recipients and examine the f
actors predictive of restenosis.
Background: Coronary graft disease (CGD) is the main factor responsible for
late graft loss. Medical treatment, surgical revascularization, or retrans
plantation gives only suboptimal results in this regard. Therefore, PTCA ha
s been attempted in this situation.
Methods: More than 332 heart transplantations in our institution have been
performed since 1992, the date of the first PTCA in our patients. We are cu
rrently in charge of 450 patients. All the characteristics, procedure-relat
ed information, and clinical outcome of patients needing PTCA were assessed
by review of each patient's clinical records. Ail coronary angiograms were
reviewed by an independent cardiologist.
Results: Since 1992, 53 coronary sites have been dilated in the course of 3
9 procedures in 29 patients. Indication for PTCA was asymptomatic angiograp
hic coronary graft disease in 35 sites (64.8%), angina in 9 (16.6%), silent
ischemia in 2 (3.7%), acute myocardial infarction in 1 (1.8%), and CHF in
7 (12.9%). Primary success (<50% residual stenosis) was obtained in 50 (94.
3%) of 53 lesions. No periprocedural death occurred. Procedural complicatio
ns were 1, transient acute renal failure and 1 persistent bleeding at the p
uncture site. Six months restenosis rate (defined as percent stenosis >50%)
was 32.5% (14/43). Mean follow-up was 1.27 year +/- 1.2 (SD). Five deaths
(17.2%) occurred in follow-up and were all in relation to coronary graft di
sease. Mean time separating PTCA from death was 0.9 year +/- 1.3 (SD). We a
lso sought to look at factors predictive of restenosis. By multivariate ana
lysis, a positive recipient's serology for cytomegalovirus (CMV) before the
graft was the only factor found protective against restenosis (odds ratio
22.4; confidence interval 1.1 to 443.4).
Conclusions: PTCA in heart transplant recipients allows a high level of pri
mary success with a low periprocedural-complication rate. Restenosis rate s
eems equivalent to restenosis rate in native coronary arteries. Mortality d
uring follow-up is increased in this population and is the consequence of a
high level of coronary events. Recipient positivity for CMV before the gra
ft is associated with a protective effect from restenosis.